Target intelligence / Profile preview

Leucine-rich single-pass membrane protein 2 (LSMEM2)

Target
LSMEM2
Molecular classification
Other (single-pass transmembrane protein, Domain of Unknown Function 4714/DUF4714)
01

Overview

Leucine-rich single-pass membrane protein 2 (LSMEM2) is a leucine-rich, single-pass transmembrane protein (DUF4714 family) highly restricted to cardiomyocytes and skeletal muscle[2][1]. It localizes specifically to the intercalated discs of cardiomyocytes and to neuromuscular junctions in skeletal muscle[4]. The molecule is used as a cell-type-specific biomarker for authentic cardiomyocytes and is downregulated in failing heart tissue, suggesting its importance in normal cardiac function[1]. Its gene (C3orf45) encodes two isoforms, both biologically similar, with predicted post-translational modifications that may affect its role in cell junction organization, vesicle transport, and mitochondrial function[2][4]. Currently, its precise biological function is under investigation; however, evidence points to a role in intercellular coupling and energy metabolism, with pathology upon dysregulation in both cardiac and skeletal muscle[1][4]. There are no known direct drug interactions, but it is considered a cell surface biomarker and a potential research target for drug testing and cardiac disease modeling[1].

Other names
LSMEM2C3orf45FLJ38608leucine rich single-pass membrane protein 2
02

Biological functions

Cell-type marker for cardiomyocytesPossible role in cell–cell junctions or chemo-electro-mechanical coupling of cardiomyocytesAssociated with mitochondrial function, ATP synthesis coupled proton transport (predicted)Involved in vesicle-mediated transport (experimental)
03

Disease associations

Downregulated in failing cardiomyocytes (heart failure)Downregulated in myotubes of patients with facioscapulohumeral muscular dystrophy (FSHD)Predicted potential relevance for sepsis-induced myopathyImplicated in skeletal muscle disease pathogenesis if overexpressed
04

Safety considerations

Sensitivity to protease treatment (dissociation methods can destroy the extracellular epitope, affecting detection and research utility)Overexpression in skeletal muscle causes abnormal vesicle transport and mitochondrial aggregates
05

Biomarkers

LSMEM2 itself, used for phenotyping, selection, or identification of authentic cardiomyocytes and assessing preparation methods

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